Sulfamic acid functionalised magnetic nanoparticles: An efficient solid acid for the multicomponent condensations

Journal of Chemical Research

Volumn 36, Issue 1, 2012, Pages 52-55

  Yarahmadi, Hossein ^a   Shaterian, Hamid Reza ^a  

^a UNIVERSITY OF SISTAN AND BALUCHESTAN   (Iran)

Author keywords

Amidoalkyl naphthols; Heterogeneous catalyst; Magnetic decantation; Multicomponent reactions; Nanoparticles; Solvent free conditions; Sulfamic acid

Indexed keywords

EID: 84857329369     PISSN: 17475198     EISSN: None     Source Type: Journal    
DOI: 10.3184/174751912X13264749420957     Document Type: Article

References (39)

1. J. Zhu and H. Bienayme, Multicomponent reactions, Wiley-VCH, Weinheim, Germany, 2005.
2. A.H. Lu, E.L. Salabas and F. Schuth, Angew. Chem. Int. Ed., 2007, 46, 1222.
3. Y. Kang, L. Zhou, X. Li and J. Yuan, J. Mater. Chem., 2011, 21, 3704.
4. V. Polshttiwar, R. Luque, A. Fihri, H. Zhu, M. Bouhrara and J.-M. Basset, Chem. Rev., 2011, 111, 3036.
5. M. Sheykhan, L. Ma'mani, A. Ebrahimi and A. Heydari, J. Mol. Catal. A: Chem., 2011, 335, 253.
6. R. Cano, M. Yus and D.J. Ramon, Tetrahedron, 2011, 67, 8079.
7. T. Zeng, L. Yang, R. Hudson, G. Song, A.R. Moores and C.-J. Li, Org. Lett., 2011, 13, 442.
8. Z.-H. Zhang, H.-Y. Lu, S.-H. Yang and J.-W. Gao, J. Com. Chem., 2010, 12, 643.
9. Y. Zha, Y. Zhang, X. Wei and Z. Yao, Chinese. J. Chem., 2010, 28, 2274.
10. C.S. Gill, B.A. Price and C.W. Jones, J. Catal., 2007, 251, 145.
11. V. Polshettiwar and R.S. Varma, Tetrahedron, 2010, 66, 1091.
12. N.T.S. Phan and C.W. Jones, J. Mol. Cat. A: Chem., 2006, 253, 123.
13. A.K. Bhattacharya and K.C. Rana, Tetrahedron Lett., 2008, 49, 2598.
14. T.S. Jin, G. Sun, Y.W.; Li and T.S. Li, Green Chem., 2002, 4, 255-258.
15. B. Wang, Y. Gu, C. Luo, T. Yang, L. Yang and J. Suo, Tetrahedron Lett., 2004, 45, 3369.
16. J.S. Yadav, P.P. Rao, D. Sreenu, R.S. Rao, V.N. Kumar, K. Nagaiah and A.R. Prasad, Tetrahedron Lett., 2005, 46, 7249.
17. B. Wang, L. Yang and J. Suo, Tetrahedron Lett., 2003, 44, 5037.
18. B. Wang, Y. Gu, L. Yang, J. Suo and O. Kenichi, Catal. Lett., 2004, 96, 71.
19. M.M. Heravi, L. Ranjbar, F. Derikvand and B. Alimadadi, Mol. Divers., 2008, 12, 191.
20. M.Z. Kassaee, H. Masrouri and F. Movahedi, Appl. Catal. A. Gen., 2011, 395, 28.
21. Y.F. Wang, T. Izawa, S. Kobayashi and M. Ohono, J. Am. Chem. Soc., 1982, 104, 64.
22. A. Shen, C.L. Chen and C. Lin, J. Physiol., 1992, 35, 45.
23. M. Damodiran, N. Panneer Selvam and P.T. Perumal, Tetrahedron Lett., 2009, 50, 5474.
24. R.D. Clark, J.M. Caroon, A.F. Kluge, D.B. Repke, A.P. Roszkowski, A.M. Strosberg, S. Baker, S.M. Bitter and M.D. Okada, J. Med. Chem., 1983, 26, 657.
25. T. Dingermann, D. Steinhilber and G. Folkers, Molecular biology in medicinal chemistry, Wiley VCH., Verlag GmbH & KGaA, Weinheim, Germany, 2004.
26. H.R. Shaterian, H. Yarahmadi and M. Ghashang, Tetrahedron, 2008, 64, 1263.
27. H.R. Shaterian, H. Yarahmadi and M. Ghashang, Bioorg. Med. Chem. Lett., 2008, 18, 788.
28. H.R. Shaterian and H. Yarahmadi, Tetrahedron Lett., 2008, 49, 1297.
29. H.R. Shaterian, A. Hosseinian and M. Ghashang, Tetrahedron. Lett., 2008, 49, 5804.
30. H.R. Shaterian, A. Amirzadeh, F. Khorami and M. Ghashang, Synth. Commun., 2008, 38, 2983.
31. H.R. Shaterian and H. Yarahmadi, Arkivoc, 2008, 2, 105.
32. N.P. Selvam and P.T. Perumal, Tetrahedron Lett., 2006, 47, 7481.
33. L. Nagarapu, M. Baseeruddin, S. Apuri and S. Kantevari, Catal. Commun., 2007, 8, 1729.
34. M.M. Khodaei, A.R. Khosropour and H. Moghanian, Synlett, 2006, 6, 916.
35. B.P. Sachin, R.S. Pankajkumar, P.S. Mandar and D.S. Shriniwas, Synth. Commun., 2007, 37, 1659.
36. M. Dabiri, A.S. Delbari and A. Bazgir, Hetrocycles, 2007, 71, 543.
37. G.H. Mahdavinia, M.A. Bigdeli and M.M. Heravi, Chinese. Chem. Lett., 2008, 19, 1171.
38. B. Das, K. Laxminarayana, B. Ravikanth and B.R. Rao, J. Mol. Catal. A: Chem., 2007, 261, 180.
39. S. Kantevari, S.V.N. Vuppalapati and L. Nagarapu, Catal. Commun., 2007, 8, 1857.